These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 16374328)

  • 21. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
    Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
    Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetics of inherited retinal disease.
    Francis PJ
    J R Soc Med; 2006 Apr; 99(4):189-91. PubMed ID: 16574971
    [No Abstract]   [Full Text] [Related]  

  • 23. The role of RPE65 in inherited retinal diseases.
    Bok D
    Retina; 2005 Dec; 25(8 Suppl):S61-S62. PubMed ID: 16374341
    [No Abstract]   [Full Text] [Related]  

  • 24. Governmental, university, pharmaceutical, and foundation partnerships to advance translational research in retinal disease.
    Ryan SJ
    Retina; 2005 Dec; 25(8 Suppl):S82. PubMed ID: 16374353
    [No Abstract]   [Full Text] [Related]  

  • 25. Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
    Dubey SK; Mahalaxmi N; Vijayalakshmi P; Sundaresan P
    Mol Vis; 2015; 21():88-97. PubMed ID: 25678763
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Attitudes of patients and relatives/carers towards genetic testing for inherited retinal disease.
    Bong C; Potrata B; Hewison J; McKibbin M
    Eye (Lond); 2010 Oct; 24(10):1622-5. PubMed ID: 20577274
    [No Abstract]   [Full Text] [Related]  

  • 27. An audit of genetic testing in diagnosis of inherited retinal disorders: a prerequisite for gene-specific intervention.
    Pradhan M; Hayes I; Vincent A
    Clin Exp Ophthalmol; 2009 Sep; 37(7):703-11. PubMed ID: 19788668
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Comprehensive registration of DNA sequence variants associated with inherited retinal diseases in Leiden Open Variation Databases.
    Cremers FP; den Dunnen JT; Ajmal M; Hussain A; Preising MN; Daiger SP; Qamar R
    Hum Mutat; 2014 Jan; 35(1):147-8. PubMed ID: 24123322
    [No Abstract]   [Full Text] [Related]  

  • 29. Correspondence.
    Boon CJ; van den Born LI; Keunen JE; Bergen AA; Riemslag FC; Florijn RJ; van Schooneveld MJ
    Retina; 2015 Sep; 35(9):e57-8. PubMed ID: 26312452
    [No Abstract]   [Full Text] [Related]  

  • 30. [Guidance of Medical Care for Familial Exudative Vitreoretinopathy：Research on Rare and Intractable Diseases, Health and Labour Sciences Research Grants].
    Azuma N; Shiraga F
    Nippon Ganka Gakkai Zasshi; 2017 Jun; 121(6):487-97. PubMed ID: 30088717
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Reply: To PMID 25545482.
    Fung AT; Yzer S; Allikmets R
    Retina; 2015 Sep; 35(9):e58. PubMed ID: 26312453
    [No Abstract]   [Full Text] [Related]  

  • 32. [Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge].
    Ďuďáková Ľ; Kousal B; Kolářová H; Hlavatá L; Lišková P
    Cesk Slov Oftalmol; 2016; 72(4):128-136. PubMed ID: 27860478
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis.
    Hiraoka M; Trese MT; Shastry BS
    Hum Genet; 1999 Jun; 104(6):526-7. PubMed ID: 10453744
    [No Abstract]   [Full Text] [Related]  

  • 34. [Gene therapy of eye diseases].
    Sakamoto T
    Fukuoka Igaku Zasshi; 2002 Oct; 93(10):204-7. PubMed ID: 12471718
    [No Abstract]   [Full Text] [Related]  

  • 35. Mirror image of familial exudative vitreoretinopathy in identical twins.
    Teke MY; Tekin K; Aydemir E; Yavrum F
    Int Ophthalmol; 2019 Apr; 39(4):935-941. PubMed ID: 29492729
    [TBL] [Abstract][Full Text] [Related]  

  • 36.
    Guziewicz KE; Cideciyan AV; Beltran WA; Komáromy AM; Dufour VL; Swider M; Iwabe S; Sumaroka A; Kendrick BT; Ruthel G; Chiodo VA; Héon E; Hauswirth WW; Jacobson SG; Aguirre GD
    Proc Natl Acad Sci U S A; 2018 Mar; 115(12):E2839-E2848. PubMed ID: 29507198
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy.
    Wivestad Jansson R; Berland S; Bredrup C; Austeng D; Andréasson S; Wittström E
    Ophthalmic Genet; 2016 Jun; 37(2):183-93. PubMed ID: 26333019
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathy.
    Vieira V; de la Houssaye G; Dansault A; Perez E; Roche O; Dufier JL; Marsac C; Menasche M; Abitbol M
    Hum Genet; 2007 Jun; 121(5):650. PubMed ID: 17879448
    [No Abstract]   [Full Text] [Related]  

  • 39. Familial congenital grouped albinotic retinal pigment epithelial spots.
    Arana LA; Sato M; Arana J
    Arch Ophthalmol; 2010 Oct; 128(10):1362-4. PubMed ID: 20938009
    [No Abstract]   [Full Text] [Related]  

  • 40. Recent advances in the molecular basis of inherited photoreceptor degeneration.
    Clarke G; Héon E; McInnes RR
    Clin Genet; 2000 May; 57(5):313-29. PubMed ID: 10852366
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.